A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225391



Internal ID20792431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4658701..4684400hg38UCSC Ensembl
chr9:4658701..4684400hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3825700
hg1925700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6434094
Supporting Variants
Samples
Known GenesCDC37L1, PPAPDC2, SPATA6L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225391
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00023


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